rs10986769
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs10986769(A;G) |
Make rs10986769(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 125460061 |
Gene | MAPKAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs10986769 |
dbSNP (classic) | rs10986769 |
ClinGen | rs10986769 |
ebi | rs10986769 |
HLI | rs10986769 |
Exac | rs10986769 |
Gnomad | rs10986769 |
Varsome | rs10986769 |
LitVar | rs10986769 |
Map | rs10986769 |
PheGenI | rs10986769 |
Biobank | rs10986769 |
1000 genomes | rs10986769 |
hgdp | rs10986769 |
ensembl | rs10986769 |
geneview | rs10986769 |
scholar | rs10986769 |
rs10986769 | |
pharmgkb | rs10986769 |
gwascentral | rs10986769 |
openSNP | rs10986769 |
23andMe | rs10986769 |
SNPshot | rs10986769 |
SNPdbe | rs10986769 |
MSV3d | rs10986769 |
GWAS Ctlg | rs10986769 |
GMAF | 0.0629 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals